Carvedilol 51655-0713
Product NDC
51655-0713- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 28, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA078384
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Carvedilol | 3.125 mg/1 |
Drug Class
alpha-Adrenergic Blocker [EPC]beta-Adrenergic Blocker [EPC]Adrenergic alpha-Antagonists [MoA]
Packaging Options(2)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-713-25)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-713-52)